- An
enamine is an
unsaturated compound derived by the
condensation of an
aldehyde or
ketone with a
secondary amine.
Enamines are
versatile intermediates...
- The
Stork enamine alkylation involves the
addition of an
enamine to a
Michael acceptor (e.g., an α,β -unsaturated
carbonyl compound) or
another electrophilic...
- pattern. Non-carbon
nucleophiles such as water, alcohols, amines, and
enamines can also
react with an α,β-unsaturated
carbonyl in a 1,4-addition. Some...
- reactions. In 1963, G.
Stork reported the
first enamine alkylation reaction for
ketones -
Stork enamine alkylation reaction. In 1976,
Meyers reported the...
-
aldehydes toward nucleophilic addition by
formation of
enamines (e.g. used in the
Stork enamine alkylation):
International Union of Pure and
Applied Chemistry...
-
Nitrogen Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate...
-
colorless liquid. It is
classified as an
enamine.
Primary and
secondary enamines tend to isomerize, but
tertiary enamines are
kinetically stable. One unusual...
- is
widely used to
convert ketones to
enamines.
Enamines derived from
piperidine are
substrates in the
Stork enamine alkylation reaction. Upon treatment...
-
electron delocalisation with the
indole ring.[citation needed] LSD also has
enamine-type
reactivity because of the electron-donating
effects of the indole...
-
titanium tetrachloride. In the
Stork enamine alkylation,
secondary amines form
enamines when
exposed to ketones.
These enamines then
react (possibly enantioselectively)...
